Clinical trial · Interventional
Study of STRO-001, an Anti-CD74 Antibody Drug Conjugate, in Patients With Advanced B-Cell Malignancies
A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-001, an Anti-CD74 Antibody Drug Conjugate, in Patients With Advanced B-Cell Malignancies
NCT03424603CI-TRIAL-00077880completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
First-in-human Phase 1 trial to study the safety, pharmacokinetics and preliminary efficacy of STRO-001 given intravenously every 3 weeks.
Conditions
Conditions (8)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| B-cell Lymphoma | B-Cell Malignant Neoplasm | CURATED_BROADER | 0.80 |
| B Cells--Tumors | — | UNRESOLVED | — |
| Diffuse Large B Cell Lymphoma | Diffuse Large B-Cell Lymphoma | CURATED_BROADER | 0.80 |
| Follicular Lymphoma | Follicular Lymphoma | ONTOLOGY_EXACT | 0.98 |
| Indolent Lymphoma | Indolent Non-Hodgkin Lymphoma | ALIAS | 0.90 |
| Mantle Cell Lymphoma | Mantle Cell Lymphoma | ONTOLOGY_EXACT | 0.98 |
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
| Non Hodgkin Lymphoma | Non-Hodgkin Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| STRO-001 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- STRO-001
- description
- intravenous
- interventionNames
- Drug: STRO-001
Primary outcomes (4)
- measure
- Part 1: Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability of STRO-001)
- timeFrame
- 18 months
- description
- Incidence of adverse events (AEs) observed across STRO-001 dose levels
- measure
- Part 1: Define the recommended phase 2 dose (RP2D) and maximum tolerated dose (MTD) of STRO-001
- timeFrame
- 18 months
- description
- Frequency of dose-limiting toxicity and exposure across STRO-001 dose levels
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria: 1. Confirmation of diagnosis 2. Relapsed or relapsed/refractory disease 3. Age ≥ 18 years 4. ECOG performance status (0-2) 5. Life expectancy \> 3 months 6. Adequate bone marrow and renal functions 7. QTcF \<500 msec 8. Ability to comply with treatment, PK and test schedules 9. NHL only- at least one measurable lesion Key Exclusion Criteria: 1. Active plasma cell leukemia and/or leukemic manifestations of lymphoma 2. Known amyloidosis (MM patients) 3. Chronic lymphocytic leukemia and Richter's transformation, and prolymphocytic leukemia (NHL subjects) 4. T-cell malignancy 5. Sensory or motor neuropathy ≥ grade 2 6. Chronic or ongoing active infectious disease requiring systemic treatment such as, but not limited to, chronic renal infection, chronic chest infection with bronchiectasis, tuberculosis and active hepatitis C 7. Ongoing immunosuppressive therapy, including systemic corticosteroids. Note: Subjects may be using topical or inhaled corticosteroids. 8. Clinically significant cardiac disease 9. Significant concurrent, uncontrolled medical condition 10. History or clinical signs of meningeal or active CNS involvement 11. Known severe chronic obstructive pulmonary disease or asthma 12. History of significant cerebrovascular disease 13. Known Human Immunodeficiency Virus seropositivity 14. Positive serology for hepatitis B defined by a positive test for HBsAg 15. Concurrent participation in another therapeutic treatment trial 16. High screening liver function tests 17. Prior treatment with CD74 targeting therapy
References
Publications (0)
Data not yet available
No reference posted for this study.